A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3695054



Internal ID18646649
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:112431790..112627148hg38UCSC Ensembl
Innerchr9:115194070..115389428hg19UCSC Ensembl
Innerchr9:114233891..114429249hg18UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg38195359
hg19195359
hg18195359
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1051625
Supporting Variants
Samples
Known GenesHSDL2, KIAA1958
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3695054
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer